BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 1389561)

  • 1. [Clinical and histochemical findings in spinal muscular atrophy].
    Fukunaga H; Moritoyo T; Okubo R; Higuchi I; Osame M
    No To Shinkei; 1992 Jun; 44(6):547-52. PubMed ID: 1389561
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinal muscular atrophy: survival pattern and functional status.
    Chung BH; Wong VC; Ip P
    Pediatrics; 2004 Nov; 114(5):e548-53. PubMed ID: 15492357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R; Hagmann A; Boltshauser E; Moser H
    Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.
    Ben Hamida C; Soussi-Yanicostas N; Butler-Browne GS; Bejaoui K; Hentati F; Ben Hamida M
    Muscle Nerve; 1994 Apr; 17(4):400-10. PubMed ID: 8170486
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Neonatal muscular spinal atrophy: a case report].
    Pavone P; Velardita M; Trigilia T; Luca G; Lucenti C; Romeo G; Falsaperla R
    Pediatr Med Chir; 2004; 26(2):139-41. PubMed ID: 15700740
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.
    Melki J; Abdelhak S; Sheth P; Bachelot MF; Burlet P; Marcadet A; Aicardi J; Barois A; Carriere JP; Fardeau M
    Nature; 1990 Apr; 344(6268):767-8. PubMed ID: 1970420
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Electrophysiological findings in childhood spinal muscular atrophies.
    Hausmanowa-Petrusewicz I
    Rev Neurol (Paris); 1988; 144(11):716-20. PubMed ID: 3231960
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A clinical and genetic study of spinal muscular atrophy.
    Mishra VN; Kalita J; Kesari A; Mitta B; Shankar SK; Misra UK
    Electromyogr Clin Neurophysiol; 2004; 44(5):307-12. PubMed ID: 15378871
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications.
    Rudnik-Schöneborn S; Röhrig D; Morgan G; Wirth B; Zerres K
    Am J Med Genet; 1994 May; 51(1):70-6. PubMed ID: 8030672
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spinal muscular atrophy.
    Iannaccone ST
    Semin Neurol; 1998; 18(1):19-26. PubMed ID: 9562664
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Anatomoclinical correlations of spinal muscular atrophy in infancy].
    Rufo Campos M; Chinchón Lara I; Arias León E; Martínez López A; Gómez de Terreros I
    Neurologia; 1993 Mar; 8(3):105-9. PubMed ID: 8448040
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Infantile spinal muscular atrophy].
    Barois A; Estournet B; Duval-Beaupère G; Bataille J; Leclair-Richard D
    Rev Neurol (Paris); 1989; 145(4):299-304. PubMed ID: 2660222
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
    Gilliam TC; Brzustowicz LM; Castilla LH; Lehner T; Penchaszadeh GK; Daniels RJ; Byth BC; Knowles J; Hislop JE; Shapira Y
    Nature; 1990 Jun; 345(6278):823-5. PubMed ID: 1972783
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Spinal muscular atrophy in young infants].
    Smit LM; Hageman EG
    Tijdschr Kindergeneeskd; 1989 Jun; 57(3):102-6. PubMed ID: 2799798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype.
    Dubowitz V
    Eur J Paediatr Neurol; 1999; 3(2):49-51. PubMed ID: 10700538
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.
    Brzustowicz LM; Lehner T; Castilla LH; Penchaszadeh GK; Wilhelmsen KC; Daniels R; Davies KE; Leppert M; Ziter F; Wood D
    Nature; 1990 Apr; 344(6266):540-1. PubMed ID: 2320125
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood].
    Distefano G; Sciacca P; Parisi MG; Parano E; Smilari P; Marletta M; Fiumara A
    Pediatr Med Chir; 1994; 16(2):125-8. PubMed ID: 8078785
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Werdnig-Hoffmann's congenital spinal atrophy in nursing infants].
    Kutafin IuF; Osipov SM; Osipov ES
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):15-8. PubMed ID: 1646528
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
    Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R
    Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861
    [No Abstract]   [Full Text] [Related]  

  • 20. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB; Cornblath DR
    Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.